Literature DB >> 26164827

Multimodal Imaging of Central Retinal Disease Progression in a 2-Year Mean Follow-up of Retinitis Pigmentosa.

Tharikarn Sujirakul1, Michael K Lin2, Jimmy Duong3, Ying Wei3, Sara Lopez-Pintado3, Stephen H Tsang4.   

Abstract

PURPOSE: To determine the rate of progression and optimal follow-up time in patients with advanced-stage retinitis pigmentosa (RP) comparing the use of fundus autofluorescence imaging and spectral-domain optical coherence tomography.
DESIGN: Retrospective analysis of progression rate.
METHODS: Longitudinal imaging follow-up in 71 patients with retinitis pigmentosa was studied using the main outcome measurements of hyperautofluoresent ring horizontal diameter and vertical diameter along with ellipsoid zone line width from spectral-domain optical coherence tomography. Test-retest reliability and the rate of progression were calculated. The interaction between the progression rates was tested for sex, age, mode of inheritance, and baseline measurement size. Symmetry of left and right eye progression rate was also tested.
RESULTS: Significant progression was observed in >75% of patients during the 2-year mean follow-up. The mean annual progression rates of ellipsoid zone line and hyperautofluorescent ring horizontal diameter and vertical diameter were 0.45 degree (4.9%), 0.51 degree (4.1%), and 0.42 degree (4.0%), respectively. The ellipsoid zone line width and hyperautofluorescent ring horizontal diameter and vertical diameter had low test-retest variabilities of 8.9%, 9.5%, and 9.6%, respectively. This study is the first to demonstrate asymmetrical structural progression rate between right and left eye, which was found in 19% of patients. The rate of progression was significantly slower as the disease approached the fovea, supporting the theory that RP progresses in an exponential fashion. No significant interaction between progression rate and patient age, sex, or mode of inheritance was observed.
CONCLUSIONS: Fundus autofluorescence and optical coherence tomography detect progression in patients with RP reliably and with strong correlation. These parameters may be useful alongside functional assessments as the outcome measurements for future therapeutic trials. Follow-up at 1-year intervals should be adequate to efficiently detect progression.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 26164827      PMCID: PMC4754981          DOI: 10.1016/j.ajo.2015.06.032

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  56 in total

1.  Unilateral retinitis pigmentosa occurring in an individual with a germline mutation in the RP1 gene.

Authors:  Rajarshi Mukhopadhyay; Graham E Holder; Anthony T Moore; Andrew R Webster
Journal:  Arch Ophthalmol       Date:  2011-07

2.  Test-retest reliability of the multifocal electroretinogram and humphrey visual fields in patients with retinitis pigmentosa.

Authors:  William Seiple; Colleen J Clemens; Vivienne C Greenstein; Ronald E Carr; Karen Holopigian
Journal:  Doc Ophthalmol       Date:  2004-11       Impact factor: 2.379

3.  Progressive constriction of the hyperautofluorescent ring in retinitis pigmentosa.

Authors:  Luiz H Lima; Tomas Burke; Vivienne C Greenstein; Chai Lin Chou; Wener Cella; Lawrence A Yannuzzi; Stephen H Tsang
Journal:  Am J Ophthalmol       Date:  2011-12-03       Impact factor: 5.258

4.  Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-up.

Authors:  Anthony G Robson; Eva Lenassi; Zubin Saihan; Vy A Luong; Fred W Fitzke; Graham E Holder; Andrew R Webster
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-09-14       Impact factor: 4.799

5.  Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutations.

Authors:  Eliot L Berson; Bernard Rosner; Carol Weigel-DiFranco; Thaddeus P Dryja; Michael A Sandberg
Journal:  Invest Ophthalmol Vis Sci       Date:  2002-09       Impact factor: 4.799

6.  Natural history and retinal structure in patients with Usher syndrome type 1 owing to MYO7A mutation.

Authors:  Eva Lenassi; Zubin Saihan; Valentina Cipriani; Polona Le Quesne Stabej; Anthony T Moore; Linda M Luxon; Maria Bitner-Glindzicz; Andrew R Webster
Journal:  Ophthalmology       Date:  2013-11-05       Impact factor: 12.079

7.  Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2.

Authors:  Ana Fakin; Martina Jarc-Vidmar; Damjan Glavač; Crystel Bonnet; Christine Petit; Marko Hawlina
Journal:  Vision Res       Date:  2012-09-18       Impact factor: 1.886

8.  Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.

Authors:  Michael A Sandberg; Bernard Rosner; Carol Weigel-DiFranco; Terri L McGee; Thaddeus P Dryja; Eliot L Berson
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-07-18       Impact factor: 4.799

9.  Kinetics of visual field loss in Usher syndrome Type II.

Authors:  Alessandro Iannaccone; Stephen B Kritchevsky; Maria Laura Ciccarelli; Salvatore A Tedesco; Claudio Macaluso; William J Kimberling; Grant W Somes
Journal:  Invest Ophthalmol Vis Sci       Date:  2004-03       Impact factor: 4.799

Review 10.  Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update.

Authors:  Anthony G Robson; Michel Michaelides; Zubin Saihan; Alan C Bird; Andrew R Webster; Anthony T Moore; Fred W Fitzke; Graham E Holder
Journal:  Doc Ophthalmol       Date:  2007-11-06       Impact factor: 2.379

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  42 in total

1.  Correlation between B-scan optical coherence tomography, en face thickness map ring and hyperautofluorescent ring in retinitis pigmentosa patients.

Authors:  Vitor K L Takahashi; Júlia T Takiuti; Ruben Jauregui; Christine L Xu; Jimmy K Duong; Luiz H Lima; Stephen H Tsang
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2019-05-02       Impact factor: 3.117

2.  Multimodal imaging of the carriers of choroideremia and X-linked retinitis pigmentosa.

Authors:  Jin Yang; Lin-Ni Wang; Rong-Guo Yu; Li-Ying Hu; Xue Gong; Lu Chen; Bo-Jie Hu; Xiao-Rong Li; Zhi-Qing Li
Journal:  Int J Ophthalmol       Date:  2018-10-18       Impact factor: 1.779

3.  Progress of macular atrophy during 30 months' follow-up in a patient with spinocerebellar ataxia type1 (SCA1).

Authors:  Ayane Hirose; Satoshi Katagiri; Takaaki Hayashi; Tomokazu Matsuura; Norihiro Nagai; Kaoru Fujinami; Takeshi Iwata; Kazushige Tsunoda
Journal:  Doc Ophthalmol       Date:  2020-07-09       Impact factor: 2.379

Review 4.  Lessons learned from quantitative fundus autofluorescence.

Authors:  Janet R Sparrow; Tobias Duncker; Kaspar Schuerch; Maarjaliis Paavo; Jose Ronaldo Lima de Carvalho
Journal:  Prog Retin Eye Res       Date:  2019-08-28       Impact factor: 21.198

5.  Quantitative Comparison of Near-infrared Versus Short-wave Autofluorescence Imaging in Monitoring Progression of Retinitis Pigmentosa.

Authors:  Ruben Jauregui; Karen Sophia Park; Jimmy K Duong; Janet R Sparrow; Stephen H Tsang
Journal:  Am J Ophthalmol       Date:  2018-07-24       Impact factor: 5.258

6.  Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain-Optical Coherence Tomography.

Authors:  Amir H Hariri; Hong Yang Zhang; Alexander Ho; Peter Francis; Richard G Weleber; David G Birch; Frederick L Ferris; SriniVas R Sadda
Journal:  JAMA Ophthalmol       Date:  2016-06-01       Impact factor: 7.389

7.  Symmetric Age Association of Retinal Degeneration in Patients with CLN2-Associated Batten Disease.

Authors:  Kyle D Kovacs; Samir Patel; Anton Orlin; Keunpyo Kim; Sherri Van Everen; Therese Conner; Dolan Sondhi; Stephen M Kaminsky; Donald J D'Amico; Ronald G Crystal; Szilárd Kiss
Journal:  Ophthalmol Retina       Date:  2020-01-22

8.  Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

Authors:  Jason Charng; Artur V Cideciyan; Samuel G Jacobson; Alexander Sumaroka; Sharon B Schwartz; Malgorzata Swider; Alejandro J Roman; Rebecca Sheplock; Manisha Anand; Marc C Peden; Hemant Khanna; Elise Heon; Alan F Wright; Anand Swaroop
Journal:  Hum Mol Genet       Date:  2016-12-15       Impact factor: 6.150

9.  Clinical trial design for neuroprotection in RHO autosomal dominant retinitis pigmentosa; outcome measure considerations.

Authors:  Benjamin Otte; Chris Andrews; Gabrielle Lacy; Kari Branham; David C Musch; Kanishka T Jayasundera
Journal:  Ophthalmic Genet       Date:  2021-01-06       Impact factor: 1.803

10.  Spectrum of Disease Severity in Nonsyndromic Patients With Mutations in the CEP290 Gene: A Multicentric Longitudinal Study.

Authors:  Francesco Testa; Andrea Sodi; Sabrina Signorini; Valentina Di Iorio; Vittoria Murro; Raffaella Brunetti-Pierri; Enza Maria Valente; Marianthi Karali; Paolo Melillo; Sandro Banfi; Francesca Simonelli
Journal:  Invest Ophthalmol Vis Sci       Date:  2021-07-01       Impact factor: 4.799

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